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KONAN MEDICAL, INC. · Model CD-15 · UDI-DI 04582275250404

NQE
1
510(k) clearances
0
Adverse events
2
Recalls
10
Facilities

Recalls

DateFirmReason
2019-02-25Nidek, Inc.The electromagnetic noise exceeded the upper limit of the Electromagnetic Compatibility Standard (EMC: IEC 60601-1-2)
2016-08-08Nidek IncSoftware version 1.08 and 1.09 for the Specular Microscope CEM 530 included a change of analysis results feature that was not reviewed and approved by the FDA.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.